Tri- and tetra-substituted naphthalene diimides as potent G-quadruplex ligands.
Data(s) |
01/03/2008
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Resumo |
A series of tri- and tetra-substituted naphthalene diimides have been designed and synthesized. Several compounds show exceptional affinity for telomeric G-quadruplex DNA in classical and competition FRET assays and SPR studies. They inhibit telomerase in the TRAP assay, and show potent senescence-based short-term anti-proliferative effects on MCF7 and A549 cancer cell lines, and localize in the nucleus and particularly the nucleolus of MCF7 cells. |
Identificador | |
Idioma(s) |
eng |
Direitos |
info:eu-repo/semantics/restrictedAccess |
Fonte |
Cuenca , F , Greciano , O , Gunaratnam , M , Haider , S , Munnur , D , Nanjunda , R , Wilson , W D & Neidle , S 2008 , ' Tri- and tetra-substituted naphthalene diimides as potent G-quadruplex ligands. ' Bioorganic & Medicinal Chemistry Letters , vol 18(5) , no. 5 , pp. 1668-1673 . DOI: 10.1016/j.bmcl.2008.01.050 |
Palavras-Chave | #/dk/atira/pure/subjectarea/asjc/1300/1303 #Biochemistry #/dk/atira/pure/subjectarea/asjc/1300/1312 #Molecular Biology #/dk/atira/pure/subjectarea/asjc/1600/1605 #Organic Chemistry #/dk/atira/pure/subjectarea/asjc/3000/3002 #Drug Discovery #/dk/atira/pure/subjectarea/asjc/3000/3003 #Pharmaceutical Science |
Tipo |
article |